Muscular Dystrophy Association

Last updated
Muscular Dystrophy Association
AbbreviationMDA
FormationJune 1950;74 years ago (1950-06)
FounderPaul Cohen
Founded at New York City, U.S.
Type non-profit
13-1665552
Focuspatient services, disease research, care and advocacy
Location
Region
United States
Key people
  • Donald S. Wood (CEO) [1]
  • Former Governor Brad Henry (Chairman) [2]
  • Sharon Hesterlee, Ph.D. (Chief Research Officer) [3]
Revenue
$63.7 million (in 2020) [4]
Website www.mda.org

Muscular Dystrophy Association (MDA) is an American nonprofit organization dedicated to supporting people living with muscular dystrophy, ALS, and related neuromuscular diseases. Founded in 1950 by Paul Cohen, who lived with muscular dystrophy, MDA accelerates research, advances care, and works to empower families to live longer and more independent lives [5] [6] but is perhaps known for its working relationship with comedian, actor and entertainer Jerry Lewis, its national chairman and number one volunteer of 55 years and host of his annual telethon held each Labor Day weekend live on-air. [7] The organization's headquarters is in Chicago, Illinois. [8]

Contents

History

The organization was founded in 1950 by a group with personal connections to muscular dystrophy, including Paul Cohen who lived with the disease. [9] Originally known as the Muscular Dystrophy Associations of America, it was renamed to its present name in the 1970s. [7]

In 1954, MDA began its partnership with the International Association of Fire Fighters for its annual Fill the Boot fundraising drive. [10] In 1955, the organization held its first summer camp. [11]

In 1980, American motorcycle manufacturer Harley Davidson became an MDA National Sponsor; [12] in 1987 the MDA Ride For Life program began, a fundraising motorcycle ride held over Labor Day weekend. [13] In 1986, oil and gas provider Citgo became a second national sponsor of the organization. [14]

In 1982, the MDA Shamrocks program launched in Grand Rapids, Michigan, and became a national program one year later. [15] In 1996, MDA and Lewis were jointly honored by the American Medical Association with a lifetime achievement awards for their contributions to the health and welfare of humanity. [16]

Dr. Stanley Appel established Houston Methodist Hospital's amyotrophic lateral sclerosis clinic with MDA in 1982, which has evolved into the MDA ALS Research and Clinical Center at the Houston Methodist Neurological Institute. Dr. Appel's pioneering work includes the development of an immunotherapy treatment that may slow the progression of ALS. Dr. Appel's efforts were recognized by the MDA when he received the MDA's Tribute Award in 2022. [17]

In October 2020, the MDA Telethon, which had originally run from 1966 to 2014, was reimagined as The MDA Kevin Hart Kids Telethon after a six-year hiatus. [18] The two-hour event was held virtually due to the COVID-19 pandemic, and streamed live on the Laugh Out Loud network and its YouTube channel. [19] Celebrity guests for the 2020 telethon included Jack Black, Josh Gad, Michael B. Jordan, and Jillian Mercado. [20]

In November 2020, MDA launched a tool, called the neuroMuscular ObserVational Research (MOVR) Visualization and Reporting Platform (VRP), to help make clinical data more accessible and accelerate discovery of muscular dystrophy treatments. [21]

In response to the COVID-19 pandemic, MDA converted several of its traditional programs to virtual formats and introduced new virtual programming. The latter included several Facebook Live events discussing challenges that the pandemic placed on people with disabilities. [22] [23] It also provided COVID-19 resources and recommendations for neuromuscular patients and providers via its online resource center. [24] Throughout stay at home orders due to the COVID-19 pandemic, MDA shared a "joke of the day" from National Ambassador Ethan Lybrand via their social media channels. [25]

In January 2021, MDA announced NFL running back Nyheim Hines as its national spokesperson. [26]

The Muscular Dystrophy Association (MDA) was established to lead research and support for individuals affected by muscular dystrophy and related diseases.

In a recent [interview](https://denver-frederick.com/2024/01/12/the-muscular-dystrophy-association-reimagined-a-chat-with-mdas-dr-donald-wood/) with Denver Frederick, Dr. Donald Wood, the current CEO of MDA, discussed the organization's founding legacy and its evolving role in reimagining support and research for the muscular dystrophy community. Dr. Wood highlighted MDA's commitment to continuing the vision of its founders through expanded programs and initiatives.

Awards

Research!America Advocacy Award (2025) [27]

In 2025, MDA received the Research!America Advocacy Award in recognition of its work in research and advocacy for neuromuscular diseases.

Institutional Awards

  MDA received this prestigious award for its advocacy and leadership in neuromuscular disease research and care. [28] 
  Awarded to MDA's Gene Therapy Support Network for its contributions to advancing gene therapy initiatives. [29] 
  Recognized for MDA’s publication, *Quest Media Print*, showcasing efforts in communicating with patients and families. [30] 
  Awarded to MDA for excellence in public service within the scientific community. [31]

Team/Group Awards

  • **Top 100 Marketing Teams - OnConference (2024)**
  Acknowledging MDA’s Marketing and Communications team for their innovative strategies. [32]
  • **Drive Purpose Campaign - PR Daily Content Marketing Awards (2024)**
  For the #AccessibleAirTravel campaign that advocates for accessibility in air travel. [33]
  • **Call to Action - 16th Annual Shorty Award Finalist and Audience Honor**
  Recognized for the #AccessibleAirTravel campaign, promoting accessibility awareness. [34]
  • **Call to Action – 9th Annual Shorty Award Finalist**
  Acknowledging the impactful messaging of the #AccessibleAirTravel campaign. [35]
  • **Federal Advocacy by a Patient Advocate or Organization - EveryLife Foundation RareVoice Awards (2023)**
  Honoring MDA’s advocacy leaders Mindy Henderson and Madison Lawson for their impactful work. [36]
  • **Communications Innovation Award - Public Affairs Council Innovation Awards (2024)**
  Recognizing the #AccessibleAirTravel campaign for innovative communications strategies. [37]

Individual Awards

  • **Most Valuable Philanthropist Award - Major League Baseball Players Association (2024)**
  Rhys Hoskins, an MDA advocate, received this award for his philanthropic efforts. [38]
  • **Marvin Miller Man of the Year Award - Major League Baseball Players Association (2024)**
  Awarded to Rhys Hoskins for his advocacy on behalf of MDA. [39]
  • **The Top 50 Women Chief Development Officers of 2024 – Women We Admire**
  Ruth Ann Daily, MDA's Chief Development Officer, received this honor for her leadership in philanthropy. [40]
  • **Top Women in Marketing - Ragan Team Leaders (2024)**
  Morgan Roth, MDA’s Chief Marketing Officer, was recognized for her strategic contributions to marketing. [41]
  • **Top 50 Chief Operations Officer - OnConference (2024)**
  Mike Kennedy, MDA’s Chief Financial Officer and Chief Operating Officer, was honored for his operational excellence. [42]
  • **Henry Viscardi Achievement Award (2023)**
  Awarded to Mindy Henderson, MDA’s Vice President of Disability Outreach & Empowerment, for her contributions to advocacy. [43]
  • **Marcoms Most Influential List - The PRNet (2023)**
  Mary Fiance, MDA’s Vice President of Strategic Communications, was recognized for her influence in communications. [44]

National Ambassador

MDA has a tradition of selecting National Ambassadors who are people living with neuromuscular disease. [45] Since the program's inception in 1952, over 45 National Ambassadors have shared their experiences to emphasize the need for funding research and developing treatments and cures for neuromuscular diseases. [46] [47] These representatives engage with partners, volunteers, supporters, and notable figures, gaining exposure through social media channels and national media outlets. Former youth ambassadors have pursued diverse fields in adulthood, advocating for improvements in accessibility, early intervention treatments through newborn screening, and advancements in research and care for MDA families and individuals living with disabilities. MDA's National Ambassadors were formerly known as "National Goodwill Ambassadors", which, until the 1980s, were referred to as "poster children". In 1952, the MDA inaugurated Michael Danna as its first Poster Child. [48]

One of the most well-known ambassadors was Mattie Stepanek, the National Goodwill Ambassador from 2002 until his death in 2004, notable for his best-selling Heartsongs series of poetry books, and his appearances on The Oprah Winfrey Show and Good Morning America. [49] Another notable ambassador is Ethan LyBrand, who has Duchenne muscular dystrophy and gained national recognition for his Shorty Award-winning "Joke-A-Day for MDA" campaign during the COVID-19 pandemic. [50]

Research

In 1986, MDA-funded researcher Louis M. Kunkel identified the dystrophin gene, the gene for Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD). [51] MDA funded the first gene therapy trial in 1999, followed by the first vector based gene therapy trial for DMD in 2006. [52]

In 2007, MDA funded Adrian R. Krainer and his colleagues at the Cold Spring Harbor Laboratory in Laurel Hollow, New York for the early-stage development of nusinersen. Nusinersen became FDA approved in 2016 as the first treatment for spinal muscular dystrophy (SMA). [53]

As of 2018, MDA had a total funding commitment of more than $58 million distributed among 312 research grants. [54] By 2019, MDA supported 252 research projects worldwide, totaling a funding commitment of more than $66 million. [55]

MDA is actively involved in supporting the development of gene therapies for rare neuromuscular diseases. In 2023, the association introduced the Kickstart Program to lower the barriers for gene therapy development. The program assembles a team of experts to collaboratively assist selected projects, positioning them for follow-on grant funding. The Kickstart Program was presented at the 2023 MDA Clinical & Scientific Conference, where discussions focused on opportunities to de-risk gene therapies, current barriers to development, collaborative frameworks, and data management. [3]

MDA supported the FDA's decision in 2023 to approve an experimental gene therapy developed by Sarepta Therapeutics that aims to slow the progression of Duchenne muscular dystrophy by facilitating the production of a protein called micro-dystrophin in patients' muscles. [56] Advancements in Duchenne muscular dystrophy treatment have prompted MDA to lobby for newborn screening panels for early detection and treatment initiation. [57]

Programs and events

Fire fighters raising money for MDA as part of the Fill the Boot Drive in Clinton, Michigan Fire Fighters raising money for Muscular Dystrophy Association Clinton Michigan.JPG
Fire fighters raising money for MDA as part of the Fill the Boot Drive in Clinton, Michigan

Fill the Boot Drive

During National Boot Day, the MDA partners with the International Association of Fire Fighters (IAFF) to launch Fill the Boot fundraising events. These events help support research, care, and advocacy for families affected by muscular dystrophy, ALS, and related neuromuscular diseases in the United States. The partnership between MDA and IAFF dates back to 1954, with IAFF designating MDA as its charity of choice. Firefighters across the country have raised $690 million over nearly seven decades, leading to breakthroughs in research, FDA-approved treatments, and advocacy efforts such as access to care and newborn screening. [58]

MDA's annual payments to IAFF, which ranged from $980,000 to $1.4 million between 2015 and 2020 according to U.S. Department of Labor filings, received some scrutiny for their size relative to the charity's expenditures. [59]

Telethon

Debuting in 1966 and held annually on Labor Day weekend until 2014, the telethon was originally hosted by veteran film star, comedian and singer Jerry Lewis, who also served as the MDA's national chairman since its inception in 1950 and hosted the show until 2010. In 2005, the MDA made the unprecedented decision to pledge $1 million of the telethon's money raised to Hurricane Katrina disaster relief, making the donation specifically to the Salvation Army (though the telethon also urged viewers to give to the American Red Cross). In 2008, the annual televised fundraiser raised a record $65,031,393.

Official MDA logo used until January 29, 2016 Official MDA Logo.png
Official MDA logo used until January 29, 2016

Originally broadcast for up to 21½ hours from 1966 to 2010, the event was cut back to six hours in 2011. [60] The 2011 edition of the telethon was originally announced to have been Lewis' last as host, with him continuing his role as national chairman; [61] however, on August 3, 2011, the MDA announced that Lewis resigned as host and chairman, due to circumstances not revealed. [62] However, in 2016, one year before his death, Lewis broke a five-year silence in a video endorsing MDA's redesigned web site and brand, declaring that the work to end muscular dystrophy be continued.

Additionally, Lewis' support was so ironclad over the years that children and adults assisted by MDA are referred to as Jerry's Kids. From 2012 to 2014, the show was known as the MDA Show of Strength . In early 2015, the organization announced it was discontinuing the show. [63]

On September 9, 2020, MDA executives announced plans to relaunch their annual MDA telethon with a new host, comedian Kevin Hart. [64] Entitled The MDA Kevin Hart Kids Telethon, the new two-hour telethon was seen exclusively through participating social media platforms; the event was broadcast October 24, 2020, at 8 p.m. EDT. [65] The special was a dual-charity event, with proceeds going towards both MDA and "Help From The Hart", an organization founded by the aforementioned new host of the program. Hart's charity announced that it will use its portion of funds raised to "support education, health and social needs programs targeting underserved communities and servicing youth through education scholarships." [66] The telethon was accompanied by a 10-hour Let's Play livestream, called Let's Play For A Cure, which featured DJ and producer Zedd, gaming personality missharvey and esports athletes. [67] The livestream was a part of a week-long "streamathon", which featured esports stars playing games including League of Legends , Rocket League, Fortnite , Call of Duty and Fall Guys . [68]

Following the Kevin Hart Kids Telethon was MDA's 70th Anniversary Show, hosted by entertainment TV journalists Nancy O'Dell and Jann Carl. [67]

MDA Clinical & Scientific Conference

The MDA Clinical & Scientific Conference is a prominent event that gathers over 2,000 professionals, including scientists and clinicians, specializing in neuromuscular diseases. The conference showcases research, fosters collaborations, and promotes the latest advancements in the field. It covers various aspects of research, from pre-clinical to clinical, and supports the development of improved care and treatment for the neuromuscular community. The conference also hosts the Annual Insights in Research Investment Summit, which focuses on research and investment stakeholders in neuromuscular diseases. The 2023 conference featured a keynote address by Dr. Peter Marks, director of the FDA's Center for Biologics Evaluation and Research, on the growing impact of gene therapies in treating rare disorders. [69]

Quest Media

MDA publishes a quarterly magazine, Quest, catering to people with neuromuscular diseases and their caretakers. Mindy Henderson, diagnosed with type 2 spinal muscular atrophy (SMA) and a patient advocate, is the editor-in-chief as of 2023. The magazine, with a circulation of around 100,000, extends its reach through distribution at neurologists' offices and the MDA's network of 150 care centers across the country. Besides focusing on science and research, Quest's coverage includes adaptive lifestyles, travel, medical equipment, accessible fashion, employment, and media representation. [70]

MDA Summer Camp

Every summer, for one week, thousands of children from across the country who have been diagnosed with neuromuscular diseases are able to attend a camp designated for only them. MDA Summer Camp offers children and young adults the opportunity to participate in recreational activities that foster independence, self-confidence, skill development, and friendships. There is a one counselor to one camper ratio and the entire week the children, ages 8–17, are paired with an adult volunteer. They participate in activities and games and stay overnight. [71] The camps are set up locally and are different weeks throughout the months of May through August. The entire camp staff are volunteer members and are required to interview and apply with good recommendations. The camp is offered at no cost to campers and their families; [72] the cost of the camp for the campers and volunteers is covered by the many fundraisers the MDA does each year. [73]

Official MDA Muscle Walk logo since 2016 MDA Muscle Walk 2016.png
Official MDA Muscle Walk logo since 2016

Muscle Walk

Started in 2010, the MDA Muscle Walk is an annual 1 to 3.1 mile lap event held in over 150 communities across the United States to raise money for research and patient services. [74] In 2022, MDA resumed in-person Muscle Walks in numerous locations, including Phoenix, Chicago, St. Louis, Detroit, Boston, Twin Cities, Houston, and Dallas, while continuing to offer a virtual Muscle Walk option to enhance participation flexibility. [75] [76]

Shamrocks retail fundraising campaign

Throughout February and March, retailers across the US contribute to the MDA Shamrocks campaign, the largest St. Patrick's Day fundraising initiative in the country. They provide customers with the opportunity to either round up their purchases or donate a specific amount, such as $1, $3, or $5. Customers can write their names on paper shamrocks, which are then displayed in stores to show support for MDA's mission to empower people with neuromuscular diseases to lead longer, more independent lives. [15] [77]

Care Center Network

MDA's Care Center Network is recognized as the largest network of multidisciplinary clinics specializing in neuromuscular diseases in the United States, with over 150 clinics distributed throughout the country. In addition to offering specialized care, these centers are also active sites of research. [78]

In 2023, MDA expanded its Resource Center by launching the Gene Therapy Support Network. This network provides resources and guidance about approved gene therapies for people living with neuromuscular diseases, aiming to help the community navigate the complexities of emerging gene therapies. Clinical networking through the MDA Care Center Network contributes additional support by facilitating best practice sharing between different care centers. [79]

Diseases targeted

MDA targets a wide range of neuromuscular diseases, including muscular dystrophies, motor neuron diseases, ion channel diseases, mitochondrial diseases, myopathies, neuromuscular junction diseases, and peripheral nerve diseases. Specific examples include Duchenne muscular dystrophy (DMD), a severe form of muscular dystrophy, ALS (amyotrophic lateral sclerosis), and Charcot–Marie–Tooth disease (CMT), which impacts peripheral nerves.

MDA also addresses numerous rare disorders, such as Andersen–Tawil syndrome, Laing distal myopathy, and Walker–Warburg syndrome. Additionally, the association covers conditions like Becker muscular dystrophy (BMD), congenital muscular dystrophies (CMD), myotonic dystrophy (DM), spinal muscular atrophy (SMA), and myasthenia gravis (MG). [80]

Legislation

MDA supported the Newborn Screening Saves Lives Reauthorization Act of 2013 (H.R. 1281; 113th Congress), a bill that would amend the Public Health Service Act to reauthorize grant programs and other initiatives to promote expanded screening of newborns and children for heritable disorders. [81] The MDA argued that "many of the drug therapies currently under development for MDA's community will be of most benefit if administered either presymptomatically or early in the progression of the disease. Thus, for some of the diseases in MDA's program, the availability of a newborn screening program at the time of treatment availability presents the best opportunity for impacting optimal and potential lifesaving treatment outcomes." [82]

MDA supported the Paul D. Wellstone Muscular Dystrophy Community Assistance, Research and Education Amendments of 2013 (H.R. 594; 113th Congress), a bill that would amend the Public Health Service Act to revise the muscular dystrophy research program of the National Institutes of Health (NIH). [83] MDA argued that "a great deal of work still needs to be done, and increased federal support is needed to ensure that researchers can continue making progress toward finding a cure." [84]

In December 2021, President Joe Biden signed the Accelerating Access to Critical Therapies for ALS Act into law. The act aimed to speed up the development and approval of therapies for ALS and other neuromuscular diseases. During the signing ceremony President Biden acknowledged the Muscular Dystrophy Association for playing a crucial role in advocating for the legislation. [85]

In May 2024, MDA supported the reauthorization of the Federal Aviation Administration (FAA) through a $105 billion bill passed by Congress. The legislation includes improvements in air travel accessibility for people with disabilities, representing significant progress in this area. [86]

Independent charity assessments

MDA is recognized by the Better Business Bureau's Wise Giving Alliance as an accredited charity that meets all 20 Standards for Charity Accountability. As of the year ending December 31, 2022, MDA reported significant funding directed towards patient and community services, professional public health education, and research. The organization's financial activities, leadership compensation, and fundraising methods are transparently disclosed, emphasizing their commitment to accountability and ethical practices. [87]

Charity Navigator, which is the largest independent evaluator of charities, gives MDA two out of four stars based on Financial, Accountability, and Transparency Performance Metrics. [88] In 2019, CharityWatch gave MDA a grade of D, citing many financial issues in the organization. [89]

MDA has received the Candid Platinum Seal of Transparency from GuideStar, recognizing its commitment to transparency and accountability. [90]

Criticism

MDA and Lewis have been criticized by disability rights activists for their tendency to paint disabled people as, these advocates say, "pitiable victims who want and need nothing more than a big charity to take care of or cure them." [91]

Related Research Articles

<span class="mw-page-title-main">Muscular dystrophy</span> Diseases in which skeletal muscle breaks down over time

Muscular dystrophies (MD) are a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown of skeletal muscles over time. The disorders differ as to which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin. Some types are also associated with problems in other organs.

<span class="mw-page-title-main">Limb–girdle muscular dystrophy</span> Muscular degenerative disorder primarily of the hip and shoulders

Limb–girdle muscular dystrophy (LGMD) is a genetically heterogeneous group of rare muscular dystrophies that share a set of clinical characteristics. It is characterised by progressive muscle wasting which affects predominantly hip and shoulder muscles. LGMD usually has an autosomal pattern of inheritance. It currently has no known cure or treatment.

<span class="mw-page-title-main">Duchenne muscular dystrophy</span> Type of muscular dystrophy

Duchenne muscular dystrophy (DMD) is a severe type of muscular dystrophy predominantly affecting boys. The onset of muscle weakness typically begins around age four, with rapid progression. Initially, muscle loss occurs in the thighs and pelvis, extending to the arms, which can lead to difficulties in standing up. By the age of 12, most individuals with Duchenne muscular dystrophy are unable to walk. Affected muscles may appear larger due to an increase in fat content, and scoliosis is common. Some individuals may experience intellectual disability, and females carrying a single copy of the mutated gene may show mild symptoms.

<span class="mw-page-title-main">Becker muscular dystrophy</span> Genetic muscle disorder

Becker muscular dystrophy (BMD) is an X-linked recessive inherited disorder characterized by slowly progressing muscle weakness of the legs and pelvis. It is a type of dystrophinopathy. The cause is mutations and deletions in any of the 79 exons encoding the large dystrophin protein, essential for maintaining the muscle fiber's cell membrane integrity. Becker muscular dystrophy is related to Duchenne muscular dystrophy in that both result from a mutation in the dystrophin gene, however the hallmark of Becker is milder in-frame deletions. and hence has a milder course, with patients maintaining ambulation till 50–60 years if detected early.

<span class="mw-page-title-main">Oculopharyngeal muscular dystrophy</span> Medical condition

Oculopharyngeal muscular dystrophy (OPMD) is a rare form of muscular dystrophy with symptoms generally starting when an individual is 40 to 50 years old. It can be autosomal dominant neuromuscular disease or autosomal recessive. The most common inheritance of OPMD is autosomal dominant, which means only one copy of the mutated gene needs to be present in each cell. Children of an affected parent have a 50% chance of inheriting the mutant gene.

Jann Carl is a co-host and part owner of the syndicated TV show Small Town Big Deal. Carl and her co-host, Rodney K. Miller, report on uplifting stories about people, places and events throughout communities big and small across the United States. The show first aired on September 6, 2012, on the RFD-TV cable network. Small Town Big Deal has aired almost 100 episodes since 2012 and is now viewed on network and local television stations in nearly 80 percent of the United States.

Muscular Dystrophy Canada (MDC) is a non-profit organization seeking a cure for neuromuscular disorders. Founded in 1954 as Muscular Dystrophy Association of Canada, volunteers and staff nationwide have helped to provide support and resources to those affected. Since the founding year, over $64 million has been put towards research via collaborations, fundraising events, and donations.

<span class="mw-page-title-main">Facioscapulohumeral muscular dystrophy</span> Muscular degenerative disease of the face, shoulder blades, and upper arms

Facioscapulohumeral muscular dystrophy (FSHD) is a type of muscular dystrophy, a group of heritable diseases that cause degeneration of muscle and progressive weakness. Per the name, FSHD tends to sequentially weaken the muscles of the face, those that position the scapula, and those overlying the humerus bone of the upper arm. These areas can be spared, and muscles of other areas usually are affected, especially those of the chest, abdomen, spine, and shin. Almost any skeletal muscle can be affected in advanced disease. Abnormally positioned, termed 'winged', scapulas are common, as is the inability to lift the foot, known as foot drop. The two sides of the body are often affected unequally. Weakness typically manifests at ages 15–30 years. FSHD can also cause hearing loss and blood vessel abnormalities at the back of the eye.

Neuromuscular medicine is a subspecialty of neurology and physiatry that focuses the diagnosis and management of neuromuscular diseases. The field encompasses issues related to both diagnosis and management of these conditions, including rehabilitation interventions to optimize the quality of life of individuals with these conditions. This field encompasses disorders that impact both adults and children and which can be inherited or acquired, typically from an autoimmune disease. A neurologist or physiatrist can diagnose these diseases through a clinical history, examination, and electromyography including nerve conduction studies. Many recent drug therapies have been developed to address the acquired neuromuscular diseases including but not limited to immune suppression and drugs that increase the neurotransmitters at the neuromuscular junction. Gene modifying therapies are also a recent treatment branch of neuromuscular medicine with advancements made in disorders such as spinal muscular atrophy and Duchenne muscular dystrophy. 

Robert Ross (1920–2006) was the founder and leader of the Muscular Dystrophy Association in 1950. Ross was CEO for 44 years until his death in 2006. The Muscular Dystrophy Association is an organization which combats muscular dystrophy and diseases of the nervous system and muscular system in general by funding research, providing medical and community services, and educating health professionals and the general public. The work of Robert Ross was appreciated by many and it was he who persuaded Jerry Lewis to undertake a yearly telethon to raise money for muscular dystrophy. Starting in February 1999, Ross wrote a column for MDA, titled The Ross Report—the final submission to The Ross Report was made in May 2006, one month before Ross's death.

<i>The Jerry Lewis MDA Labor Day Telethon</i> American telethon

The MDA Labor Day Telethon was an annual telethon held on Labor Day in the United States to raise money for the Muscular Dystrophy Association (MDA). The Muscular Dystrophy Association was founded in 1950 with hopes of gaining the American public's interest. The show was hosted by comedian, actor, singer and filmmaker Jerry Lewis from its 1966 inception until 2010. The history of MDA's telethon dates back to the 1950s, when the Jerry Lewis Thanksgiving Party for MDA raised funds for the organization's New York City area operations. The telethon was held annually on Labor Day weekend beginning in 1966, and raised $2.45 billion for MDA from its inception through 2009.

<span class="mw-page-title-main">ALS Therapy Development Institute</span>

The ALS Therapy Development Institute is a non-profit biotechnology research organization focused on finding treatments for amyotrophic lateral sclerosis (ALS). With a staff including more than 30 scientists, it operates a research and development program centered on ALS.

Augustine L. Nieto II was the founder and chief executive of Life Fitness, as well as the chairman of Augie's Quest to Cure ALS, and the ALS Therapy Development Institute. He and his wife, Lynne, lived in Corona Del Mar, California, and had four children and eight grandchildren.

Laura Ann Hershey was a poet, journalist, popular speaker, feminist, and a disability rights activist and consultant. Known to have parked her wheelchair in front of buses, Hershey was one of the leaders of a protest against the paternalistic attitudes and images of people with disabilities inherent to Jerry Lewis's MDA Telethon. She was a regular columnist for the Christopher and Dana Reeve Foundation, and on her own website, Crip Commentary, and was published in a variety of magazines and websites. She was admired for her wit, her ability to structure strong arguments in the service of justice, and her spirited refusal to let social responses to her spinal muscular atrophy define the parameters of her life as anything less than a full human existence. She was also the mother of an adopted daughter.

Bryson Foster is a noted teen activist who advocates and fundraises for the development of treatments for muscular dystrophy.

<span class="mw-page-title-main">Charlotte Sumner</span> American neurologist

Charlotte Jane Sumner is an American neurologist. She is a professor in the Departments of Neurology and Neuroscience at Johns Hopkins School of Medicine. Dr. Sumner cares for patients with genetically mediated neuromuscular diseases and directs a laboratory focused on developing treatments for these diseases. She co-directs the Johns Hopkins Muscular Dystrophy Association Care Center, the Spinal Muscular Atrophy (SMA), and the Charcot-Marie-Tooth (CMT) clinics, which deliver multidisciplinary clinical care, engage in international natural history studies, and provide therapeutics.

Toshifumi (Toshi) Yokota is a biomedical scientist and professor of medical genetics at the University of Alberta, holding the titles of the Friends of Garrett Cumming Research & Muscular Dystrophy Canada Endowed Research Chair and the Henri M. Toupin Chair in Neurological Science. Yokota is widely recognized for pioneering work in antisense therapy for muscular dystrophy and other genetic diseases, which led to the development of viltolarsen, an FDA-approved treatment for Duchenne muscular dystrophy (DMD). With over 100 peer-reviewed publications and several patents, Yokota has made significant contributions to the field of precision medicine. Yokota also co-edited three volumes in the Methods in Molecular Biology series by Humana Press, Springer-Nature and serves on editorial boards of multiple scientific journals.

<span class="mw-page-title-main">Casimersen</span> Medication

Casimersen, sold under the brand name Amondys 45, is an antisense oligonucleotide medication used for the treatment of Duchenne muscular dystrophy (DMD) in people who have a confirmed mutation of the dystrophin gene that is amenable to exon 45 skipping. It is an antisense oligonucleotide of phosphorodiamidate morpholino oligomer (PMO). Duchenne muscular dystrophy is a rare disease that primarily affects boys. It is caused by low levels of a muscle protein called dystrophin. The lack of dystrophin causes progressive muscle weakness and premature death.

SGT-003 is an experimental gene therapy being tested for Duchenne's muscular dystrophy. It is hoped to be an improvement on Solid Bioscience's earlier gene therapy SGT-001.

Stephen Donald Wilton, also known as Steve Wilton, is an Australian molecular biologist and academic, serving as the Foundation Professor of Molecular Therapy at Murdoch University and adjunct professor at the University of Western Australia (UWA). He also fulfills dual roles as a Director at the Perron Institute for Neurological and Translational Science and deputy director at Murdoch's Centre for Molecular Medicine and Innovative Therapeutics (CMMIT).

References

  1. ↑ Miller, Hawken (17 November 2020). "Q&A: Meet Donald Wood, the Muscular Dystrophy Association's New CEO and President". Muscular Dystrophy News. Retrieved 19 April 2021.
  2. ↑ "Muscular Dystrophy Association Elects Governor Brad Henry as Chairman and Christopher Rosa, Ph.D. as Vice Chairman of the Board of Directors". GlobeNewswire (Press release). 9 January 2023. Retrieved 2023-08-18.
  3. 1 2 "New MDA Program for Gene Therapy Development in Ultra-Rare Diseases: Sharon Hesterlee, PhD". Neurology Live. 24 March 2023. Retrieved 2023-08-18.
  4. ↑ "Muscular Dystrophy Association". ProPublica. 9 May 2013. Retrieved 2023-08-18.
  5. ↑ "VIDEO: Frank Sinatra Backstage at the Jerry Lewis Telethon Circa 1970s". Reel Life With Jane. 6 September 2015. Retrieved 2023-08-18.
  6. ↑ "Lou Gehrig Day". MLB.com. Retrieved 2023-08-18.
  7. 1 2 "History". Muscular Dystrophy Association. 29 December 2015.
  8. ↑ "MDA to Move HQ to Chicago". Globest.com. Retrieved 2023-08-18.
  9. ↑ Huang, Binghui (2017-09-02). "Jerry Lewis' work pays off in new drugs for muscular dystrophy". The Morning Call.
  10. ↑ "Cleveland Firefighters raise over $40,000 for MDA". The Place. Retrieved 2021-06-11.
  11. ↑ Cook, B.W. (2011-07-29). "The Crowd: Fundraiser helps summer camp programs". Daily Pilot. Retrieved 2021-06-11.
  12. ↑ Staff, U. M. C. (2009-09-11). "Harley-Davidson contributes $4.5M to MDA". Ultimate Motorcycling. Retrieved 2021-06-11.
  13. ↑ PhD, Patricia Inacio (September 2020). "Virtual Events Mark MDA's Muscular Dystrophy Awareness Month" . Retrieved 2021-06-11.
  14. ↑ Burgeson, John (2016-12-19). "CITGO-sponsored golf tourney raises $100k for MD". Connecticut Post. Retrieved 2021-06-11.
  15. 1 2 Barker, John (25 March 2013). "Kroger Customers Support MDA's Shamrocks Program". Patch.
  16. ↑ "Jerry Lewis: Biography". KTRE.com. 26 August 2003. Retrieved 2021-06-11.
  17. ↑ "At 89, Houston Methodist Dr. Stanley Appel still at forefront of ALS research". Houston Chronicle. Retrieved 2023-08-18.
  18. ↑ Strub, Chris. "After Six-Year Hiatus, Reimagined MDA Kevin Hart Kids Telethon Returns October 24". Forbes. Retrieved 2021-06-11.
  19. ↑ Miller, Hawken (20 October 2020). "MDA Telethon Returning, Going Virtual With Host Kevin Hart" . Retrieved 2021-06-11.
  20. ↑ Clolery, Paul. "MDA Getting Back In The Telethon Game". The NonProfit Times. Retrieved 2021-06-11.
  21. ↑ Ray, Dr. Forest (12 November 2020). "MDA Launches Tool to Make Clinical Data More Accessible to Researchers" . Retrieved 2021-04-23.
  22. ↑ Wexler, Marisa (2 April 2020). "MDA Hosting Online Q&A on COVID-19 Today". ALS News Today. Retrieved 29 September 2021.
  23. ↑ Wexler, Marisa (6 August 2020). "MD Advocates Offer Advice for Students With Neuromuscular Disorders Amid COVID-19". Muscular Distrophy. Retrieved 29 September 2021.
  24. ↑ Meglio, Marco (29 April 2021). "Apic Bio plans to initiate a phase 1/2 clinical trial in late 2021 or early 2022 as a multi-center, 3-part study to evaluate APB-102 in patients with SOD1-ALS mutations". Neurology Live. Retrieved 29 September 2021.
  25. ↑ Waterfiled, Sophia (24 April 2020). "Fifth-Grader Tells a Joke a Day to Keep Americans Laughing During Coronavirus Pandemic". Newsweek. Retrieved 29 September 2021.
  26. ↑ Tannebaum, Taylor (11 February 2021). "Colts RB Nyheim Hines named national spokesperson for MDA". wthr.com. Retrieved 2021-07-07.
  27. ↑ "Research!America Advocacy Awards to Recognize Nation's Outstanding Leaders for Medical and Health Research". Research!America. 2025. Retrieved 2024-11-07.
  28. ↑ [Research!America Advocacy Awards to Recognize Nation's Outstanding Leaders for Medical and Health Research](https://www.researchamerica.org/press-releases-statements/researchamerica-advocacy-awards-to-recognize-nations-outstanding-leaders-for-medical-and-health-research/)
  29. ↑ [Advanced Therapies Awards 2024](https://advancedtherapiesawards.phacilitate.com/winners/)
  30. ↑ [PR Daily Awards 2024](https://www.prdaily.com/pr-daily-awards-and-top-agencies-finalists-and-honorees-announced-see-the-full-list/#Print%20Publication)
  31. ↑ [American Society of Gene + Cell Therapy Award](https://www.asgct.org/awards/annual-meeting-awards/sonia-skarlatos-public-service-award)
  32. ↑ [OnConference 2024](https://www.onconferences.com/24-coo-winners)
  33. ↑ [PR Daily Content Marketing Awards 2024](https://www.prdaily.com/congratulations-to-the-winners-of-pr-dailys-social-media-digital-content-marketing-awards/)
  34. ↑ [Shorty Awards 16th Annual](https://shortyawards.com/16th/winners)
  35. ↑ [Shorty Awards 9th Annual](https://shortyawards.com/9th-impact/finalists/)
  36. ↑ [EveryLife Foundation RareVoice Awards 2023](https://everylifefoundation.org/rare-advocates/rarevoice-awards-2020/rarevoice-awards-recipients/)
  37. ↑ [Public Affairs Council Innovation Awards 2024](https://pac.org/innovation-award-winners-in-communications-grassroots-and-lobbying-honored-at-the-advocacy-conference)
  38. ↑ [MLB Players Choice Awards 2024](https://www.mlb.com/news/players-choice-awards-2024)
  39. ↑ [MLB Players Choice Awards 2024](https://www.mlb.com/news/players-choice-awards-2024)
  40. ↑ [Women We Admire 2024](https://thewomenweadmire.com/2024/09/12/the-top-50-women-chief-development-officers-of-2024/)
  41. ↑ [Ragan Team Leaders 2024](https://www.prdaily.com/pr-daily-announces-the-top-women-in-marketing-class-of-2024-honorees/#Team%20Leaders)
  42. ↑ [OnConference 2024](https://www.onconferences.com/24-coo-winners)
  43. ↑ [The Viscardi Center 2023](https://viscardicenter.org/2023-henry-viscardi-achievement-awards-recipients-announced/#:~:text=The%202023%20Henry%20Viscardi%20Achievement,%E2%80%9D%20Zografopoulos%2C%20Z%20Life%2C%20U.S.)
  44. ↑ [The PRNet 2023](https://theprnet.com/journals/the-pr-net-mmi-awards)
  45. ↑ "Ira Walker, living with SMA type 2, named MDA National Ambassador". smanewstoday.com. 12 January 2024. Retrieved 2024-05-31.
  46. ↑ "Meet Reagan Imhoff, National Goodwill Ambassador for MDA". Medium. 16 February 2017. Retrieved 2023-08-18.
  47. ↑ "Muscular Dystrophy Association Announces 2023 National Ambassador Leah Zelaya from New York". Yahoo Finance. 23 January 2023. Retrieved 2023-08-18.
  48. ↑ "MDA National Ambassadors Share the Everyday Impact of Neuromuscular Disease". Mobility Works. 6 February 2020. Retrieved 2023-08-18.
  49. ↑ "Matthew 'Mattie' Stepanek, 13; Poet, Peacemaker". Los Angeles Times. 24 June 2004. Retrieved 2023-08-18.
  50. ↑ "Decatur youth featured in ad debuting during Oscars". AL.com. 25 April 2021. Retrieved 2023-08-18.
  51. ↑ Weidman Burke, Chelsea. "The Time for DMD Gene Therapy is Now: A Chat with the MDA". BioSpace. Retrieved 2021-07-07.
  52. ↑ Agencies, United States Congress Senate Committee on Appropriations Subcommittee on Departments of Labor, Health and Human Services, Education, and Related (2001). Muscular Dystrophy: Hearing Before a Subcommittee of the Committee on Appropriations, United States Senate, One Hundred Seventh Congress, First Session, Special Hearing, February 27, 2001, Washington, DC. U.S. Government Printing Office. ISBN   978-0-16-065977-5.{{cite book}}: CS1 maint: multiple names: authors list (link)
  53. ↑ Neurology, The Lancet (2020-03-01). "Leading the way for neuromuscular disorders since 1950". The Lancet Neurology. 19 (3): 195. doi: 10.1016/S1474-4422(20)30027-2 . ISSN   1474-4422. PMID   32085828.
  54. ↑ Luxner, Larry (4 April 2019). "MDA Conference Bringing Neuromuscular Disease Experts to Orlando to Share 'New Era' in Treatment, Research". CHarcot-Marie-Tooth News. Retrieved 29 September 2021.
  55. ↑ The Lancet Neurology (2020). "Leading the way for neuromuscular disorders since 1950". The Lancet Neurology. 19 (3): 195. doi: 10.1016/S1474-4422(20)30027-2 . PMID   32085828.
  56. ↑ "FDA Approves First Gene Therapy for Duchenne Muscular Dystrophy". Time. Retrieved 2023-08-18.
  57. ↑ "UPDATE ON PPMD'S NEWBORN SCREENING EFFORTS". Parent Project Muscular Dystrophy. 31 May 2023. Retrieved 2023-08-18.
  58. ↑ "2022 IAFF Impact Report" (PDF). MDA.org. Retrieved 2023-08-18.
  59. ↑ Fitch, Marc E. (2020-10-19). "The Fitch Files: Why is the International Association of Fire Fighters getting millions from a charity?". Yankee Institute. Retrieved 2024-03-09.
  60. ↑ MDA: "MDA Labor Day Telethon Moves to Shorter Format", October 6, 2010.
  61. ↑ MDA press release, via Zap2it: "You'll Never Walk Alone: Jerry Lewis To Make His Final Telethon Appearance", May 16, 2011.
  62. ↑ MDA: "Jerry Lewis Completes Run as MDA National Chairman", August 3, 2011. Archived August 4, 2011, at the Wayback Machine
  63. ↑ "MDA ends Jerry Lewis Labor Day telethon". USA TODAY. Retrieved 2017-10-29.
  64. ↑ "Kevin Hart's Muscular Dystrophy Association Telethon Relaunch Adds to Lineup; Will Stream on LOL Network – Update". 8 October 2020.
  65. ↑ MDA Press Release: "Muscular Dystrophy Association Announces Relaunch of Iconic Telethon Hosted by Actor & Comedian Kevin Hart"
  66. ↑ "Kevin Hart to helm famed MDA telethon hosted for decades by Jerry Lewis". 9 September 2020.
  67. 1 2 Miller, Hawken (20 October 2020). "MDA Telethon Returning, Going Virtual With Host Kevin Hart" . Retrieved 2021-07-07.
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  69. ↑ "Top FDA Official Touts 'Promise of Gene Therapy' at MDA Annual Conference". Rare Disease Advisor. 21 March 2023. Retrieved 2023-08-18.
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  71. ↑ "At Special Camp, 17-Year-Old With Spinal Muscular Atrophy Gets to Swim, Play Basketball and More". Inside Edition. 30 August 2019. Retrieved 2023-08-18.
  72. ↑ Frank, Grace (7 February 2020). "From Care Centers to Summer Camp, MDA Leads in Helping Others" . Retrieved 2021-04-23.
  73. ↑ "MDA Summer Camp". Muscular Dystrophy Association. 22 December 2017.
  74. ↑ "Participate in an Event | Muscular Dystrophy Association". Muscular Dystrophy Association. 2015-12-17. Retrieved 2017-10-29.
  75. ↑ "The Muscle Walk Comes to Detroit in August". Hour Detroit. 16 March 2022. Retrieved 2023-08-18.
  76. ↑ "Muscular Dystrophy Association Announces 2022 Muscle Walks in Local Communities Nationwide to Empower Families Living with Muscular Dystrophy, ALS, and Related Neuromuscular Disease". MDA.org. 11 March 2022. Retrieved 2023-08-18.
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  78. ↑ "Dollars to help strengthen communities". Capital Press. December 2020. Retrieved 2021-04-23.
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  80. ↑ "Diseases". Muscular Dystrophy Association. 28 March 2018.
  81. ↑ "CBO - H.R. 1281". Congressional Budget Office. 6 June 2014. Retrieved 24 June 2014.
  82. ↑ "Newborn Screening Saves Lives Reauthorization Act (H.R. 1281/S. 1417)". Muscular Dystrophy Association. Archived from the original on 24 October 2013. Retrieved 24 June 2014.
  83. ↑ "H.R. 594 - Summary". United States Congress. Retrieved 30 July 2014.
  84. ↑ "MD CARE Act Update (2014)". Muscular Dystrophy Association. Archived from the original on 25 June 2014. Retrieved 31 July 2014.
  85. ↑ "Remarks by President Biden at Signing of H.R. 3537, the "Accelerating Access to Critical Therapies for ALS Act"". WhiteHouse.gov. 23 December 2021. Retrieved 2023-08-18.
  86. ↑ "Congress passed its air travel overhaul. Here's what that means for WA". The Seattle Times. 15 May 2024. Retrieved 2024-07-18.
  87. ↑ "Muscular Dystrophy Association charity review & reports by Give.org". Give.org. Retrieved 2023-08-18.
  88. ↑ "Charity Navigator - Rating for Muscular Dystrophy Association". Charity Navigator. Retrieved 2023-08-18.
  89. ↑ "Kevin Hart Aims to Reboot the MDA Telethon (And His Hosting Career)". The Hollywood Reporter . 16 October 2020.
  90. ↑ "Muscular Dystrophy Association". GuideStar. Retrieved 2024-07-18.
  91. ↑ TheKidsAreAllRight documentary website about a renegade Jerry's Kid named Mike Ervin
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